Canonical Allele Identifier: CA463017189

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145828C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133584C>G , CM000670.2:g.133133584C>G	GRCh38
NC_000008.10:g.134145828C>G , CM000670.1:g.134145828C>G	GRCh37
NC_000008.9:g.134215010C>G	NCBI36
NG_015832.1:g.271624C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8112C>G MANE Select	ENSP00000220616.4:p.Leu2704=
ENST00000220616.8:c.8112C>G	ENSP00000220616.4:p.Leu2704=
ENST00000519178.5:c.3478C>G
ENST00000519543.5:c.2511C>G	ENSP00000430430.1:p.Leu837=
ENST00000521107.1:c.324C>G	ENSP00000430161.1:p.Leu108=
ENST00000522691.1:n.198C>G
ENST00000523756.5:c.4767C>G
NM_003235.4:c.8112C>G	NP_003226.4:p.Leu2704=
XM_005251038.3:c.7920C>G	XP_005251095.1:p.Leu2640=
XM_006716622.2:c.8049C>G	XP_006716685.1:p.Leu2683=
XM_005251038.4:c.7920C>G	XP_005251095.1:p.Leu2640=
XM_006716622.3:c.8049C>G	XP_006716685.1:p.Leu2683=
XM_017013793.1:c.8046C>G	XP_016869282.1:p.Leu2682=
XM_017013794.1:c.7977C>G	XP_016869283.1:p.Leu2659=
XM_017013795.1:c.7941C>G	XP_016869284.1:p.Leu2647=
XM_017013796.1:c.7893C>G	XP_016869285.1:p.Leu2631=
XM_017013797.1:c.7851C>G	XP_016869286.1:p.Leu2617=
NM_003235.5:c.8112C>G MANE Select	NP_003226.4:p.Leu2704=